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Journal of the American College of Cardiology|August 28, 2024
Continuous Rhythm Monitoring With Implanted Loop Recorders in Children and Adolescents With Brugada SyndromeMarco Bergonti, Giuseppe Ciconte, Jose Cruzalegui Gomez, et al.
Cardiovascular Research|February 19, 2015
Role of common and rare variants in SCN10A: results from the Brugada syndrome QRS locus gene discovery collaborative studyElijah R Behr, Eleonora Savio-Galimberti, Julien Barc, et al.
European Heart Journal|March 6, 2024
Implantable loop recorders in patients with Brugada syndrome: the BruLoop studyMarco Bergonti, Frederic Sacher, Elena Arbelo, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|May 11, 2026
Ventricular conduction is a marker for arrhythmic risk in SCN5A-E1784K overlap sodium channel diseaseMichael W T Tanck, Yanushi D Wijeyeratne, Julien Barc, et al.
JACC. Clinical Electrophysiology|November 20, 2020
Genotype Predicts Outcomes in Fetuses and Neonates With Severe Congenital Long QT SyndromeJeremy P Moore, Roberto G Gallotti, Kevin M Shannon, et al.
Medrxiv : the Preprint Server for Health Sciences|February 19, 2024
Multiplexed Assays of Variant Effect and Automated Patch-clamping Improve KCNH2-LQTS Variant Classification and Cardiac Event Risk StratificationMatthew J O'Neill, Chai-Ann Ng, Takanori Aizawa, et al.
Circulation|September 24, 2024
Multiplexed Assays of Variant Effect and Automated Patch Clamping Improve KCNH2-LQTS Variant Classification and Cardiac Event Risk StratificationMatthew J O'Neill, Chai-Ann Ng, Takanori Aizawa, et al.
European Heart Journal|June 7, 2019
Calmodulin mutations and life-threatening cardiac arrhythmias: insights from the International Calmodulinopathy RegistryLia Crotti, Carla Spazzolini, David J Tester, et al.
Circulation. Genomic and Precision Medicine|November 9, 2020
SCN5A Mutation Type and a Genetic Risk Score Associate Variably With Brugada Syndrome Phenotype in SCN5A FamiliesYanushi D Wijeyeratne, Michael W Tanck, Yuka Mizusawa, et al.
European Heart Journal|August 2, 2023
Clinical presentation of calmodulin mutations: the International Calmodulinopathy RegistryLia Crotti, Carla Spazzolini, Mette Nyegaard, et al.
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